822 Results for "

CHO,

" in MedChemExpress (MCE) Product Catalog:
Products (822)

822 Results for "CHO," in MCE Product Catalog:

170
170 Publications Verification
Cat. No.: HY-P7118
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: TGF-beta-1; TGFB1; TGFB; rHuTGF-β1
Species:  
Source:  
CHO
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65
65 Cited Publications
Cat. No.: HY-K2014

MCE PEI Transfection Reagent is designed based on 25 kDa PEI. It has high-efficiency, low-toxicity, strong-stability, and is suitable for many cell types, such as HEK-293、HEK-293T、CHO-K1、COS-1、COS-7、NIH/3T3、Sf9、HepG2 and HeLa et, even some hard-to-transfect cells. It can also be applied to large-scale recombinant protein expression and virus production. The 1 mL is defined as the base specification. All larger sizes correspond to incremental volumes of this base.

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54
54 Cited Publications
Cat. No.: HY-P7080
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuIL-4; BSF-1; Binetrakin; Lymphocyte stimulatory factor 1; Pitrakinra
Species:  
Source:  
CHO
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47
47 Cited Publications
Cat. No.: HY-P1001
CAS No.: 169332-60-9
Target:  

Caspase

Research Areas:  

Cancer

Ac-DEVD-CHO is a Caspase-3 inhibitor with a Ki value of 230 pM.
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24
24 Cited Publications
Cat. No.: HY-15036
CAS No.: 15307-86-5
Purity:  99.92%
Target:  

COX Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Diclofenac is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells , and 5.1 and 0.84 μM for ovine COX-1 and COX-2, respectively . Diclofenac induces apoptosis of neural stem cells (NSCs) via the activation of the caspase cascade .
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24
24 Cited Publications
Cat. No.: HY-15038
CAS No.: 15307-81-0
Purity:  99.99%
Target:  

COX Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Diclofenac potassium is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells , and 5.1 and 0.84 μM for ovine COX-1 and COX-2, respectively . Diclofenac potassium induces apoptosis of neural stem cells (NSCs) via the activation of the caspase cascade .
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24
24 Cited Publications
Cat. No.: HY-15036A
CAS No.: 78213-16-8
Purity:  99.95%
Target:  

COX Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Diclofenac diethylamine is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells , and 5.1 and 0.84 μM for ovine COX-1 and COX-2, respectively . Diclofenac diethylamine induces apoptosis of neural stem cells (NSCs) via the activation of the caspase cascade .
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24
24 Cited Publications
Cat. No.: HY-15037
CAS No.: 15307-79-6
Purity:  99.94%
Synonyms: GP 45840
Target:  

COX Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Diclofenac Sodium (GP 45840) is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells , and 5.1 and 0.84 μM for ovine COX-1 and COX-2, respectively . Diclofenac Sodium induces apoptosis of neural stem cells (NSCs) via the activation of the caspase cascade .
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18
18 Cited Publications
Cat. No.: HY-P7114
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuR-spondin-1/RSPO1; Roof plate-specific spondin-1
Species:  
Source:  
CHO
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13
13 Cited Publications
Cat. No.: HY-P7086
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuNoggin; NOG
Species:  
Source:  
CHO
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13
13 Cited Publications
Cat. No.: HY-18964
CAS No.: 110044-82-1
Synonyms: Calpain inhibitor I; Ac-LLnL-CHO; ALLN
Target:  

Proteasome Apoptosis

Research Areas:  

Cancer

MG-101 (ALLN) is an inhibitor of cysteine proteases which inhibits calpain I, calpain II, cathepsin B and cathepsin L with Kis of 190, 220, 150 and 500 pM, respectively. MG-101 induces apoptosis and inhibits tumor growth, it can be used for the research of colon cancer .
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13
13 Cited Publications
Cat. No.: HY-16039
CAS No.: 1345614-59-6
Target:  

LPL Receptor

Research Areas:  

Inflammation/Immunology

AM095 is a selective LPA1 receptor antagonist. The IC50 for AM095 antagonism of LPA-induced calcium flux of human or mouse LPA1-transfected CHO cells is 0.025 and 0.023 μM, respectively.
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12
12 Cited Publications
Cat. No.: HY-P7051A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuNoggin; NOG
Species:  
Source:  
CHO
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11
11 Cited Publications
Cat. No.: HY-P7247
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rRtM-CSF; CSF1; MCSF
Species:  
Rat
Source:  
CHO
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10
10 Cited Publications
Cat. No.: HY-P7085A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuM-CSF; CSF-1; MGI-IM
Species:  
Source:  
CHO
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9
9 Cited Publications
Cat. No.: HY-P7033
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: rHuIL-13; NC30
Species:  
Source:  
CHO
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9
9 Cited Publications
Cat. No.: HY-P7050A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuM-CSF; CSF-1; MGI-IM
Species:  
Source:  
CHO
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9
9 Cited Publications
Cat. No.: HY-17038
CAS No.: 138112-76-2
Synonyms: S-20098
Agomelatine (S-20098) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively . Agomelatine is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native (porcine) and cloned, human 5-HT2C receptors, respectively .
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9
9 Cited Publications
Cat. No.: HY-17038A
CAS No.: 1176316-99-6
Synonyms: S-20098 hydrochloride
Agomelatine hydrochloride (S-20098 hydrochloride) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively . Agomelatine hydrochloride is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native (porcine) and cloned, human 5-HT2C receptors, respectively .
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9
9 Cited Publications
Cat. No.: HY-17038B
CAS No.: 824393-18-2
Synonyms: S-20098 L(+)-Tartaric acid
Agomelatine L(+)-Tartaric acid (S-20098 L(+)-Tartaric acid) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively . Agomelatine L(+)-Tartaric acid is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native (porcine) and cloned, human 5-HT2C receptors, respectively .
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